• Sr. Medical Writer (US Remote & Temp…

    Terumo Neuro (Aliso Viejo, CA)
    …that is making a difference in people's lives every day? We're a medical devices company that develops innovative neuroendovascular technologies for the ... documents and scientific presentations in cooperation with the Clinical, Medical , & Regulatory Affairs Teams, KOLs and...a medical writer for pharmaceutical, CRO, or medical device clients). 4. Excellent writing and… more
    Terumo Neuro (08/08/25)
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  • Medical Device

    Belcan (Pittsburgh, PA)
    Medical Device Job Number: 358762 Category: Regulatory Description: Job Title: Assembler - Medical Device Location: Pittsburgh, PA. Zip Code: 15238 ... JOB RESPONSIBILITIES: This position will assemble and support the various medical device manufacturing processes. POSITION DUTIES & RESPONSIBILITIES: *… more
    Belcan (07/19/25)
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  • Associate Director, Engineering - Medical

    Merck (Wilson, NC)
    …supporting regulatory inspections. + Experience in commercialization of high-volume medical device or combination products + Experience with injection ... Moldings, Management Process, Manufacturing Scale-Up, Mechanical Engineering, Medical Device Management, Medical Devices , Packaging Engineering,… more
    Merck (09/05/25)
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  • Sr. Manager Medical Affairs

    BD (Becton, Dickinson and Company) (San Diego, CA)
    …+ Preferred: Experience in the medical device industry or medical affairs + Preferred: Experience with infusion devices , informatics, and connected ... patient monitoring (eg, vital signs and hemodynamics), and the connectivity of these devices to support clinical outcomes. + Provides medical /clinical input to… more
    BD (Becton, Dickinson and Company) (09/07/25)
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  • Clinical Research Leader - JJMT Neurovascular

    J&J Family of Companies (Irvine, CA)
    …MDR, MEDDEV, ). . Clinical/ medical background is a plus. . Medical device experience is highly preferred. REQUIRED KNOWLEDGE, SKILLS, ABILITIES, ... Clinical R&D partners and cross-functional partners (eg Global Strategic Marketing, Medical Affairs, Regulatory Affairs, Health Economics and Market Access,… more
    J&J Family of Companies (08/27/25)
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  • Associate Director, Device Clinical…

    Takeda Pharmaceuticals (Lexington, MA)
    …+ Develop Device Clinical Development Strategy for Combination Products and Medical Devices + Develop comprehensive risk management strategies for devices ... device , or pharmaceutical industry experience + Experience with both medical devices , drug- device combination products, digital health technologies… more
    Takeda Pharmaceuticals (09/04/25)
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  • Sr. Specialist, Scientific Operations (Irvine, CA)…

    J&J Family of Companies (Irvine, CA)
    …in quality regulatory compliance, complaint handling, adverse event reporting, medical device risk management processes, and experience with common bio ... years of experience in a regulated environment including 3 years of direct experience with medical devices in the fields of technical or medical writing,… more
    J&J Family of Companies (09/05/25)
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  • Associate Director - QA - Medical

    Lilly (Indianapolis, IN)
    …approve complaint investigations associated with use, design, and manufacturing investigations for medical devices and drug/ device combination products + ... oversight for quality system activities performed by Quality Assurance in the medical device complaint handling area. To support implementation and maintenance… more
    Lilly (08/20/25)
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  • Associate Director, Device Technology

    Merck (West Point, PA)
    …Moldings, Management Process, Manufacturing Compliance, Medical Devices , Product Commercialization, Quality Management System Improvement, Regulatory ... managing external partners in the scale-up, development, commercialization, and transfer of medical devices and combination products, with a focus on… more
    Merck (09/06/25)
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  • Post Market Surveillance Analyst III

    Abbott (Burlington, MA)
    …entering information into the complaint database; independently determining and filing appropriate medical devices reports with various regulatory agencies; ... complaints. Independently assesses the complaint to determine if a medical device report needs to be filed... Reporting) + Knowledge of the use, development, and regulatory environment of medical devices more
    Abbott (08/27/25)
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